The Importance of Physiologically Relevant Cell Lines for Studying Virus-Host Interactions

被引:28
|
作者
Hare, David [1 ]
Collins, Susan [1 ]
Cuddington, Breanne [1 ]
Mossman, Karen [1 ,2 ]
机构
[1] McMaster Univ, Pathol & Mol Med, 1280 Main Str West, Hamilton, ON L8S 4L8, Canada
[2] McMaster Univ, Biochem & Biomed Sci, 1280 Main Str West, Hamilton, ON L8S 4L8, Canada
来源
VIRUSES-BASEL | 2016年 / 8卷 / 11期
关键词
primary cell; immortalized cell; interferon; interferon regulatory factor 3; interferon-stimulated genes; signal transduction; antiviral defense; INTERFERON REGULATORY FACTOR-3; TRANSCRIPTION FACTOR IRF-1; ALPHA/BETA GENE INDUCTION; CYTOSOLIC DNA SENSOR; HUMAN-DIPLOID CELLS; INNATE IMMUNITY; T-ANTIGEN; ANTIVIRAL IMMUNITY; HUMAN FIBROBLASTS; VIRAL-INFECTIONS;
D O I
10.3390/v8110297
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses interact intimately with the host cell at nearly every stage of replication, and the cell model that is chosen to study virus infection is critically important. Although primary cells reflect the phenotype of healthy cells in vivo better than cell lines, their limited lifespan makes experimental manipulation challenging. However, many tumor-derived and artificially immortalized cell lines have defects in induction of interferon-stimulated genes and other antiviral defenses. These defects can affect virus replication, especially when cells are infected at lower, more physiologically relevant, multiplicities of infection. Understanding the selective pressures and mechanisms underlying the loss of innate signaling pathways is helpful to choose immortalized cell lines without impaired antiviral defense. We describe the trials and tribulations we encountered while searching for an immortalized cell line with intact innate signaling, and how directed immortalization of primary cells avoids many of the pitfalls of spontaneous immortalization.
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页数:10
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